α,α'-Dicinnamoyl ketene cyclic S, S-acetals 4 were reacted with ethylenediamine to afford α,α'-dicinnamoyl ketene cyclic N,N-acetals 5. This process provides a new method for thesynthesis of 5 in high yiel...α,α'-Dicinnamoyl ketene cyclic S, S-acetals 4 were reacted with ethylenediamine to afford α,α'-dicinnamoyl ketene cyclic N,N-acetals 5. This process provides a new method for thesynthesis of 5 in high yield under mild conditions.展开更多
Cyclic phosphoric acid catalyzed one-pot,four component reactions of benzil,aldehydes,primary amines and ammonium acetate in refluxing ethanol were developed,giving highly substituted imidazoles in excellent yield.
1-Benzoyl-3-aryl-4-hydroxy-4-phenylimidazolidin-2-thiones can be synthesized readily from the cyclization of 1-benzoyl-3-arylthioureas with bromine-acetophenone in the presence of excess triethylamine.
文摘α,α'-Dicinnamoyl ketene cyclic S, S-acetals 4 were reacted with ethylenediamine to afford α,α'-dicinnamoyl ketene cyclic N,N-acetals 5. This process provides a new method for thesynthesis of 5 in high yield under mild conditions.
基金CAS Key Laboratory of Molecular Recognition and Function,Institute of Chemistry,Chinese Academy of Sciences for generous financial support
文摘Cyclic phosphoric acid catalyzed one-pot,four component reactions of benzil,aldehydes,primary amines and ammonium acetate in refluxing ethanol were developed,giving highly substituted imidazoles in excellent yield.
基金ProjectsupportedbytheKeyLaboratoryofOrganicSynthesisofJiangsuProvince (No .T2 10 910 3 )andCommitteeofSuzhouScienceandTechnology (No .SG 0 2 19)
文摘1-Benzoyl-3-aryl-4-hydroxy-4-phenylimidazolidin-2-thiones can be synthesized readily from the cyclization of 1-benzoyl-3-arylthioureas with bromine-acetophenone in the presence of excess triethylamine.
